Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10630331G>A , CM000679.2:g.10630331G>A | GRCh38 |
| NC_000017.10:g.10533648G>A , CM000679.1:g.10533648G>A | GRCh37 |
| NC_000017.9:g.10474373G>A | NCBI36 |
| NG_011537.1:g.31968C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002470.4:c.5414C>T MANE Select | NP_002461.2:p.Ala1805Val |
| ENST00000583535.6:c.5414C>T MANE Select | ENSP00000464317.1:p.Ala1805Val |
| NM_002470.3:c.5414C>T | NP_002461.2:p.Ala1805Val |
| ENST00000583535.5:c.5414C>T | ENSP00000464317.1:p.Ala1805Val |
| XM_011523870.1:c.5414C>T | XP_011522172.1:p.Ala1805Val |
| XM_011523870.3:c.5414C>T | XP_011522172.1:p.Ala1805Val |
| XM_011523871.1:c.5414C>T | XP_011522173.1:p.Ala1805Val |
| XM_011523871.2:c.5414C>T | XP_011522173.1:p.Ala1805Val |